A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580773



Internal ID20953844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28289677..28290780hg38UCSC Ensembl
chr17:26616703..26617806hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241002
Samples
Known GenesKRT18P55
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580773
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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